Density functional theory (DFT) calculations using the KMLYP method on a series of pincer PCP-rhodium dihydrogen complexes have been employed to model and examine the proposed mechanisms for the pincer PCP-rhodium complexes mediated hydrogenation of carbon dioxide (CO2). The relative energies of dihydrogen rotamers and dihydride isomers were evaluated together with T1 values to determine the molecular structures of these complexes. We have investigated possible pathways for the CO2 reduction processes involving the formation of rhodium dihydride species. Although the dihydrogen complexes are more stable than the corresponding dihydride isomers, the reduction of CO2 has to proceed through the dihydride structures.
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry